| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:636268-636475 | Common:4; Rare:60 | ||||
| chr16:641744-641967 | Common:3; Rare:78 | ||||
| chr16:649199-649395 | Common:2; Rare:71 | ||||
| chr16:680233-680472 | Common:2; Rare:76 | ||||
| chr16:690354-690548 | Common:3; Rare:80 | ||||
| chr16:740951-741175 | Rare:69 | ||||
| chr16:1308860-1309199 | Common:3; Rare:92 | ||||
| chr16:1309387-1309756 | Rare:140 | ||||
| chr16:1420712-1420885 | Rare:74 | ||||
| chr16:1493263-1493587 | Common:4; Rare:98 | ||||
| chr16:1533492-1533694 | Common:1; Rare:39 | ||||
| chr16:1612032-1612354 | Common:1; Rare:105; Clinvar:1 | ||||
| chr16:1706056-1706281 | Common:1; Rare:64 | ||||
| chr16:1771521-1771865 | Common:3; Rare:133 | ||||
| chr16:1772602-1772868 | Common:3; Rare:90; Clinvar (pathogenic):2 |